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Craig Chinault
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19
Cheung, Sau Wai
13
Lupski, James
12
Ou, Zhishuo
12
Patel, Ankita
12
Shaw, Chad
9
Stankiewicz, Pawel
9
Beaudet, Arthur
7
Yatsenko, Svetlana
6
Zoghbi, Huda
6
Sahoo, Trilochan
6
Lalani, Seema
5
Li, Jiangzhen
5
Bacino, Carlos
5
Cooper, Lance
5
Ferrero, GB
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All Publications
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2009: Yatsenko S A; Kruer M C; Bader P I; Corzo D; Schuette J; Keegan C E; Nowakowska B; Peacock S; Cai W W; Peiffer D A; Gunderson K L; Ou Z; Chinault A C; Cheung S W
Identification of critical regions for clinical features of distal 10q deletion syndrome.
Clinical genetics 2009;76(1):54-62.
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2009: Chinault A Craig; Shaw Chad A; Brundage Ellen K; Tang Lin-Ya; Wong Lee-Jun C
Application of dual-genome oligonucleotide array-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes.
Genetics in medicine : official journal of the American College of Medical Genetics 2009;11(7):518-26.
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2009: Yatsenko Svetlana A; Brundage Ellen K; Roney Erin K; Cheung Sau Wai; Chinault A Craig; Lupski James R
Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome.
Human molecular genetics 2009;18(11):1924-36.
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2009: Yatsenko Svetlana A; Shaw Chad A; Ou Zhishuo; Pursley Amber N; Patel Ankita; Bi Weimin; Cheung Sau Wai; Lupski James R; Chinault A Craig; Beaudet Arthur L
Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNA.
The Journal of molecular diagnostics : JMD 2009;11(3):226-37.
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2009: Jensen Daniel R; Martin Donna M; Gebarski Stephen; Sahoo Trilochan; Brundage Ellen K; Chinault A Craig; Otto Edgar A; Chaki Moumita; Hildebrandt Friedhelm; Cheung Sau Wai; Lesperance Marci M
A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies.
American journal of medical genetics. Part A 2009;149A(3):396-402.
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2009: Shchelochkov Oleg A; Li Fang-Yuan; Geraghty Michael T; Gallagher Renata C; Van Hove Johan L; Lichter-Konecki Uta; Fernhoff Paul M; Copeland Sara; Reimschisel Tyler; Cederbaum Stephen; Lee Brendan; Chinault A Craig; Wong Lee-Jun
High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGH.
Molecular genetics and metabolism 2009;96(3):97-105.
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2008: Lu Xin-Yan; Phung Mai T; Shaw Chad A; Pham Kim; Neil Sarah E; Patel Ankita; Sahoo Trilochan; Bacino Carlos A; Stankiewicz Pawel; Kang Sung-Hae Lee; Lalani Seema; Chinault A Craig; Lupski James R; Cheung Sau W; Beaudet Arthur L
Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.
Pediatrics 2008;122(6):1310-8.
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2008: Ou Zhishuo; Martin Donna M; Bedoyan Jirair K; Cooper M Lance; Chinault A Craig; Stankiewicz Pawel; Cheung Sau W
Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication of SIX1, SIX6, and OTX2 resulting from a complex chromosomal rearrangement.
American journal of medical genetics. Part A 2008;146A(19):2480-9.
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2008: Shao Lina; Shaw Chad A; Lu Xin-Yan; Sahoo Trilochan; Bacino Carlos A; Lalani Seema R; Stankiewicz Pawel; Yatsenko Svetlana A; Li Yinfeng; Neill Sarah; Pursley Amber N; Chinault A Craig; Patel Ankita; Beaudet Arthur L; Lupski James R; Cheung Sau W
Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
American journal of medical genetics. Part A 2008;146A(17):2242-51.
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2008: Shinawi Marwan; Erez Ayelet; Shardy Deborah L; Lee Brendan; Naeem Rizwan; Weissenberger George; Chinault A Craig; Cheung Sau Wai; Plon Sharon E
Syndromic thrombocytopenia and predisposition to acute myelogenous leukemia caused by constitutional microdeletions on chromosome 21q.
Blood 2008;112(4):1042-7.
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2008: Wong Lee-Jun C; Dimmock David; Geraghty Michael T; Quan Richard; Lichter-Konecki Uta; Wang Jing; Brundage Ellen K; Scaglia Fernando; Chinault A Craig
Utility of oligonucleotide array-based comparative genomic hybridization for detection of target gene deletions.
Clinical chemistry 2008;54(7):1141-8.
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2008: Patel Ankita; Kang Sung-Hae; Lennon Patrick Alan; Li Yin Feng; Rao P Nagesh; Abruzzo Lynne; Shaw Chad; Chinault Alan Craig; Cheung Sau W
Validation of a targeted DNA microarray for the clinical evaluation of recurrent abnormalities in chronic lymphocytic leukemia.
American journal of hematology 2008;83(7):540-6.
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2008: Ou Zhishuo; Kang Sung-Hae L; Shaw Chad A; Carmack Condie E; White Lisa D; Patel Ankita; Beaudet Arthur L; Cheung Sau Wai; Chinault A Craig
Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(4):278-89.
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2008: Ou Zhishuo; Berg Jonathan S; Yonath Hagith; Enciso Victoria B; Miller David T; Picker Jonathan; Lenzi Tiffanee; Keegan Catherine E; Sutton Vernon R; Belmont John; Chinault A Craig; Lupski James R; Cheung Sau Wai; Roeder Elizabeth; Patel Ankita
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.
Genetics in medicine : official journal of the American College of Medical Genetics 2008;10(4):267-77.
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2008: Shchelochkov Oleg A; Patel Ankita; Weissenberger George M; Chinault A Craig; Wiszniewska Joanna; Fernandes Priscilla H; Eng Christine; Kukolich Mary K; Sutton V Reid
Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome.
American journal of medical genetics. Part A 2008;146A(8):1042-8.
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2008: Li Likun; Abdel Fattah ElMoataz; Cao Guangwen; Ren Chengzhen; Yang Guang; Goltsov Alexei A; Chinault A Craig; Cai Wei-Wen; Timme Terry L; Thompson Timothy C
Glioma pathogenesis-related protein 1 exerts tumor suppressor activities through proapoptotic reactive oxygen species-c-Jun-NH2 kinase signaling.
Cancer research 2008;68(2):434-43.
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2008: Ben-Shachar Shay; Ou Zhishuo; Shaw Chad A; Belmont John W; Patel Millan S; Hummel Marybeth; Amato Stephen; Tartaglia Nicole; Berg Jonathan; Sutton V Reid; Lalani Seema R; Chinault A Craig; Cheung Sau W; Lupski James R; Patel Ankita
22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.
American journal of human genetics 2008;82(1):214-21.
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2007: Brunetti-Pierri N; Grange D K; Ou Z; Peiffer D A; Peacock S K G; Cooper M L; Eng P A; Lalani S R; Chinault A C; Gunderson K L; Craigen W J; Cheung S-W
Characterization of de novo microdeletions involving 17q11.2q12 identified through chromosomal comparative genomic hybridization.
Clinical genetics 2007;72(5):411-9.
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2007: Kang S-H L; Scheffer A; Ou Z; Li J; Scaglia F; Belmont J; Lalani S R; Roeder E; Enciso V; Braddock S; Buchholz J; Vacha S; Chinault A C; Cheung S W; Bacino C A
Identification of proximal 1p36 deletions using array-CGH: a possible new syndrome.
Clinical genetics 2007;72(4):329-38.
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2007: Cheung Sau W; Shaw Chad A; Scott Daryl A; Patel Ankita; Sahoo Trilochan; Bacino Carlos A; Pursley Amber; Li Jiangzhen; Erickson Robert; Gropman Andrea L; Miller David T; Seashore Margretta R; Summers Anne M; Stankiewicz Pawel; Chinault A Craig; Lupski James R; Beaudet Arthur L; Sutton V Reid
Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.
American journal of medical genetics. Part A 2007;143A(15):1679-86.
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2007: Probst Frank J; Roeder Elizabeth R; Enciso Victoria B; Ou Zhishuo; Cooper M Lance; Eng Patricia; Li Jiangzhen; Gu Yanghong; Stratton Robert F; Chinault A Craig; Shaw Chad A; Sutton V Reid; Cheung Sau Wai; Nelson David L
Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation.
American journal of medical genetics. Part A 2007;143A(12):1358-65.
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2007: Lu Xinyan; Shaw Chad A; Patel Ankita; Li Jiangzhen; Cooper M Lance; Wells William R; Sullivan Cathy M; Sahoo Trilochan; Yatsenko Svetlana A; Bacino Carlos A; Stankiewicz Pawel; Ou Zhishu; Chinault A Craig; Beaudet Arthur L; Lupski James R; Cheung Sau W; Ward Patricia A
Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.
PloS one 2007;2(3):e327.
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2006: Sahoo Trilochan; Cheung Sau Wai; Ward Patricia; Darilek Sandra; Patel Ankita; del Gaudio Daniela; Kang Sung Hae L; Lalani Seema R; Li Jiangzhen; McAdoo Sallie; Burke Audrey; Shaw Chad A; Stankiewicz Pawel; Chinault A Craig; Van den Veyver Ignatia B; Roa Benjamin B; Beaudet Arthur L; Eng Christine M
Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(11):719-27.
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2006: Ou Zhishuo; Jarmuz Malgorzata; Sparagana Steven P; Michaud Jacques; Décarie Jean-Claude; Yatsenko Svetlana A; Nowakowska Beata; Furman Patti; Shaw Chad A; Shaffer Lisa G; Lupski James R; Chinault A Craig; Cheung Sau W; Stankiewicz Pawel
Evidence for involvement of TRE-2 (USP6) oncogene, low-copy repeat and acrocentric heterochromatin in two families with chromosomal translocations.
Human genetics 2006;120(2):227-37.
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2005: Cheung Sau W; Shaw Chad A; Yu Wei; Li Jiangzham; Ou Zhishuo; Patel Ankita; Yatsenko Svetlana A; Cooper Mitchell L; Furman Patti; Stankiewicz Pawel; Lupski James R; Chinault A Craig; Beaudet Arthur L
Development and validation of a CGH microarray for clinical cytogenetic diagnosis.
Genetics in medicine : official journal of the American College of Medical Genetics 2005;7(6):422-32.
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2003: Cao Guangwen; Yang Guang; Timme Terry L; Saika Takashi; Truong Luan D; Satoh Takefumi; Goltsov Alexei; Park Sang Hee; Men Taoyan; Kusaka Nobuyuki; Tian Weihua; Ren Chengzhen; Wang Hongyu; Kadmon Dov; Cai Wei Wen; Chinault A Craig; Boone Timothy B; Bradley Allan; Thompson Timothy C
Disruption of the caveolin-1 gene impairs renal calcium reabsorption and leads to hypercalciuria and urolithiasis.
The American journal of pathology 2003;162(4):1241-8.
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2002: Ren Chengzhen; Li Likun; Goltsov Alexei A; Timme Terry L; Tahir Salahaldin A; Wang Jianxiang; Garza Laura; Chinault A Craig; Thompson Timothy C
mRTVP-1, a novel p53 target gene with proapoptotic activities.
Molecular and cellular biology 2002;22(10):3345-57.
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2002: Boggs Barbara A; Cheung Peter; Heard Edith; Spector David L; Chinault A Craig; Allis C David
Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes.
Nature genetics 2002;30(1):73-6.
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2001: Cabeza-Arvelaiz Y; Thompson T C; Sepulveda J L; Chinault A C
LAPSER1: a novel candidate tumor suppressor gene from 10q24.3.
Oncogene 2001;20(46):6707-17.
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2001: Cabeza-Arvelaiz Y; Sepulveda J L; Lebovitz R M; Thompson T C; Chinault A C
Functional identification of LZTS1 as a candidate prostate tumor suppressor gene on human chromosome 8p22.
Oncogene 2001;20(31):4169-79.
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2001: Chinault A C; Sternberg N L
Screening large-insert libraries by PCR.
Current protocols in human genetics / editorial board, Jonathan L. Haines ... [et al.] 2001;Chapter 5():Unit 5.5.
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2000: Pershouse M; Li J; Yang C; Su H; Brundage E; Di W; Biggs P J; Bradley A; Chinault A C
BAC contig from a 3-cM region of mouse chromosome 11 surrounding Brca1.
Genomics 2000;69(1):139-42.
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2000: Boggs B A; Allis C D; Chinault A C
Immunofluorescent studies of human chromosomes with antibodies against phosphorylated H1 histone.
Chromosoma 2000;108(8):485-90.
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1998: Bilyeu K; Chinault A C
Replication timing properties across the pseudoautosomal region boundary and cytogenetic band boundaries on human distal Xp.
Chromosoma 1998;107(2):105-12.
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1998: Ansari-Lari M A; Oeltjen J C; Schwartz S; Zhang Z; Muzny D M; Lu J; Gorrell J H; Chinault A C; Belmont J W; Miller W; Gibbs R A
Comparative sequence analysis of a gene-rich cluster at human chromosome 12p13 and its syntenic region in mouse chromosome 6.
Genome research 1998;8(1):29-40.
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1997: Boggs B A; Chinault A C
Analysis of DNA replication by fluorescence in situ hybridization.
Methods (San Diego, Calif.) 1997;13(3):259-70.
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1997: Chen K S; Manian P; Koeuth T; Potocki L; Zhao Q; Chinault A C; Lee C C; Lupski J R
Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome.
Nature genetics 1997;17(2):154-63.
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1997: Subramanian P S; Chinault A C
Replication timing properties of the human HPRT locus on active, inactive and reactivated X chromosomes.
Somatic cell and molecular genetics 1997;23(2):97-109.
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1996: Boggs B A; Connors B; Sobel R E; Chinault A C; Allis C D
Reduced levels of histone H3 acetylation on the inactive X chromosome in human females.
Chromosoma 1996;105(5):303-9.
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1996: Subramanian P S; Nelson D L; Chinault A C
Large domains of apparent delayed replication timing associated with triplet repeat expansion at FRAXA and FRAXE.
American journal of human genetics 1996;59(2):407-16.
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1995: Anderson K L; Baird L; Lewis R A; Chinault A C; Otterud B; Leppert M; Lupski J R
A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p.
American journal of human genetics 1995;57(6):1351-63.
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1995: Ferrero G B; Franco B; Roth E J; Firulli B A; Borsani G; Delmas-Mata J; Weissenbach J; Halley G; Schlessinger D; Chinault A C
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3.
Human molecular genetics 1995;4(10):1821-7.
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1995: Fairman J; Chumakov I; Chinault A C; Nowell P C; Nagarajan L
Physical mapping of the minimal region of loss in 5q- chromosome.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(16):7406-10.
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1995: Lee C C; Yazdani A; Wehnert M; Zhao Z Y; Lindsay E A; Bailey J; Coolbaugh M I; Couch L; Xiong M; Chinault A C
Isolation of chromosome-specific genes by reciprocal probing of arrayed cDNA and cosmid libraries.
Human molecular genetics 1995;4(8):1373-80.
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1995: Gunaratne P H; Nakao M; Ledbetter D H; Sutcliffe J S; Chinault A C
Tissue-specific and allele-specific replication timing control in the imprinted human Prader-Willi syndrome region.
Genes & development 1995;9(7):808-20.
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1995: Wang I; Franco B; Ferrero G B; Chinault A C; Weissenbach J; Chumakov I; Le Paslier D; Levilliers J; Klink A; Rappold G A
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1).
Genomics 1995;26(2):229-38.
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1994: Jayakumar A; Chirala S S; Chinault A C; Baldini A; Abu-Elheiga L; Wakil S J
Isolation and chromosomal mapping of genomic clones encoding the human fatty acid synthase gene.
Genomics 1994;23(2):420-4.
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1994: Wapenaar M C; Schiaffino M V; Bassi M T; Schaefer L; Chinault A C; Zoghbi H Y; Ballabio A
A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22.
Human molecular genetics 1994;3(7):1155-61.
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1994: Boggs B A; Chinault A C
Analysis of replication timing properties of human X-chromosomal loci by fluorescence in situ hybridization.
Proceedings of the National Academy of Sciences of the United States of America 1994;91(13):6083-7.
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1994: Nagarajan L; Zavadil J; Claxton D; Lu X; Fairman J; Warrington J A; Wasmuth J J; Chinault A C; Sever C E; Slovak M L
Consistent loss of the D5S89 locus mapping telomeric to the interleukin gene cluster and centromeric to EGR-1 in patients with 5q- chromosome.
Blood 1994;83(1):199-208.
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1994: Yen P H; Ferrero G B; Chinault A C; Mohandas T; Ballabio A
Characterization of the deletion breakpoints in a patient with steroid sulfatase deficiency.
Human mutation 1994;4(1):76-8.
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1993: Banfi S; Chung M Y; Kwiatkowski T J; Ranum L P; McCall A E; Chinault A C; Orr H T; Zoghbi H Y
Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb.
Genomics 1993;18(3):627-35.
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1993: Mutirangura A; Jayakumar A; Sutcliffe J S; Nakao M; McKinney M J; Buiting K; Horsthemke B; Beaudet A L; Chinault A C; Ledbetter D H
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene.
Genomics 1993;18(3):546-52.
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1993: Ellison K A; Roth E J; McCabe E R; Chinault A C; Zoghbi H Y
Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome.
American journal of medical genetics 1993;47(7):1124-34.
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1993: Virta-Pearlman V J; Gunaratne P H; Chinault A C
Analysis of a replication initiation sequence from the adenosine deaminase region of the mouse genome.
Molecular and cellular biology 1993;13(10):5931-42.
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1993: Lee W C; Ferrero G B; Chinault A C; Yen P H; Ballabio A
A yeast artificial chromosome contig linking the steroid sulfatase and Kallmann syndrome loci on the human X chromosome short arm.
Genomics 1993;18(1):1-6.
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1993: Wapenaar M C; Bassi M T; Schaefer L; Grillo A; Ferrero G B; Chinault A C; Ballabio A; Zoghbi H Y
The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regions.
Human molecular genetics 1993;2(7):947-52.
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1992: Kuwano A; Mutirangura A; Dittrich B; Buiting K; Horsthemke B; Saitoh S; Niikawa N; Ledbetter S A; Greenberg F; Chinault A C
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
Human molecular genetics 1992;1(6):417-25.
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1992: Guzzetta V; Franco B; Trask B J; Zhang H; Saucedo-Cardenas O; Montes de Oca-Luna R; Greenberg F; Chinault A C; Lupski J R; Patel P I
Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p.
Genomics 1992;13(3):551-9.
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1992: Gelb B D; Worley K C; Griffin L D; Adams V; Chinault A C; McCabe E R
Characterization of human genomic yeast artificial chromosome inserts containing hexokinase 1 coding information on chromosome 10.
Biochemical medicine and metabolic biology 1992;47(3):265-9.
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1992: Mutirangura A; Kuwano A; Ledbetter S A; Chinault A C; Ledbetter D H
Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15.
Human molecular genetics 1992;1(2):139.
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1992: Banfi S; Ledbetter S A; Chinault A C; Zoghbi H Y
An easy and rapid method for the detection of chimeric yeast artificial chromosome clones.
Nucleic acids research 1992;20(7):1814.
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1992: Mutirangura A; Ledbetter S A; Kuwano A; Chinault A C; Ledbetter D H
Dinucleotide repeat polymorphism at the GABAA receptor beta 3 (GABRB3) locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15.
Human molecular genetics 1992;1(1):67.
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1991: Nelson D L; Ballabio A; Victoria M F; Pieretti M; Bies R D; Gibbs R A; Maley J A; Chinault A C; Webster T D; Caskey C T
Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(14):6157-61.
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1991: Fabiny J M; Jayakumar A; Chinault A C; Barnes E M
Ammonium transport in Escherichia coli: localization and nucleotide sequence of the amtA gene.
Journal of general microbiology 1991;137(4):983-9.
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1991: Chang Z Y; Nygaard P; Chinault A C; Kellems R E
Deduced amino acid sequence of Escherichia coli adenosine deaminase reveals evolutionarily conserved amino acid residues: implications for catalytic function.
Biochemistry 1991;30(8):2273-80.
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1990: Kwiatkowski T J; Zoghbi H Y; Ledbetter S A; Ellison K A; Chinault A C
Rapid identification of yeast artificial chromosome clones by matrix pooling and crude lysate PCR.
Nucleic acids research 1990;18(23):7191-2.
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1989: Taylor K M; Shetta M; Talpaz M; Kantarjian H M; Hardikar S; Chinault A C; McCredie K B; Spitzer G
Myeloproliferative disorders: usefulness of X-linked probes in diagnosis.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(6):419-22.
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1989: Jayakumar A; Hwang S J; Fabiny J M; Chinault A C; Barnes E M
Isolation of an ammonium or methylammonium ion transport mutant of Escherichia coli and complementation by the cloned gene.
Journal of bacteriology 1989;171(2):996-1001.
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1988: Sykes R C; Lin D; Hwang S J; Framson P E; Chinault A C
Yeast ARS function and nuclear matrix association coincide in a short sequence from the human HPRT locus.
Molecular & general genetics : MGG 1988;212(2):301-9.
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1988: Lin D; Chinault A C
Comparative study of DNase I sensitivity at the X-linked human HPRT locus.
Somatic cell and molecular genetics 1988;14(3):261-72.
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1987: Smith H C; Ochs R L; Lin D; Chinault A C
Ultrastructural and biochemical comparisons of nuclear matrices prepared by high salt or LIS extraction.
Molecular and cellular biochemistry 1987;77(1):49-61.
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1987: Yoffe G; Chinault A C; Talpaz M; Blick M B; Kantarjian H M; Taylor K; Spitzer G
Clonal nature of Philadelphia chromosome-positive and -negative chronic myelogenous leukemia by DNA hybridization analyses.
Experimental hematology 1987;15(7):725-8.
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1987: Yoffe G; Spitzer G; Boggs B A; McCredie K B; Stass S A; Chinault A C
Determination of clonality in acute nonlymphocytic leukemia by restriction fragment length polymorphism and methylation analysis.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1987;1(3):226-30.
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1986: Patel P I; Framson P E; Caskey C T; Chinault A C
Fine structure of the human hypoxanthine phosphoribosyltransferase gene.
Molecular and cellular biology 1986;6(2):393-403.
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1984: Yen P H; Patel P; Chinault A C; Mohandas T; Shapiro L J
Differential methylation of hypoxanthine phosphoribosyltransferase genes on active and inactive human X chromosomes.
Proceedings of the National Academy of Sciences of the United States of America 1984;81(6):1759-63.
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